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105198

(+)-Dehydroabietylamine

Name: (+)-Dehydroabietylamine
Brand: ALDRICH

technical grade, 60%

Synonym(s):

1,4a-Dimethyl-7-isopropyl-1,2,3,4,4a,9,10,10a-octahydro-1-phenanthrenemethylamine

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About This Item

Empirical Formula (Hill Notation):

C₂₀H₃₁N

CAS Number:

1446-61-3

Molecular Weight:

285.47

UNSPSC Code:

12352116

NACRES:

NA.22

PubChem Substance ID:

24846693

EC Number:

215-899-7

Beilstein/REAXYS Number:

3084620

MDL number:

MFCD00213430

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Properties

grade

technical grade

optical activity

[α]20/D +56.1°, c = 2.4 in pyridine

composition

high molecular weight primary amines, 90%

concentration

60%

refractive index

n20/D 1.546 (lit.)

SMILES string

[H][C@@]12CCc3cc(ccc3[C@@]1(C)CCC[C@@]2(C)CN)C(C)C

InChI

1S/C20H31N/c1-14(2)15-6-8-17-16(12-15)7-9-18-19(3,13-21)10-5-11-20(17,18)4/h6,8,12,14,18H,5,7,9-11,13,21H2,1-4H3/t18-,19-,20+/m0/s1

InChI key

JVVXZOOGOGPDRZ-SLFFLAALSA-N

Description

pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Synthesis and bio-molecular study of (+)-N-Acetyl-α-amino acid dehydroabietylamine derivative for the selective therapy of hepatocellular carcinoma.

Muhammad Ayaz Mustufa et al.

BMC cancer, 16(1), 883-883 (2016-11-16)

The purpose of present work is to synthesize novel (+)-Dehydroabietylamine derivatives (DAAD) using N-acetyl-α-amino acid conjugates and determine its cytotoxic effects on hepatocellular carcinoma cells. An analytical study was conducted to explore cytotoxic activity of DAAD on hepatocellular carcinoma cell

Synthesis of Tertiary and Quaternary Amine Derivatives from Wood Resin as Chiral NMR Solvating Agents.

Tiina Laaksonen et al.

Molecules (Basel, Switzerland), 20(11), 20873-20886 (2015-11-28)

Chiral tertiary and quaternary amine solvating agents for NMR spectroscopy were synthesized from the wood resin derivative (+)-dehydroabietylamine (2). The resolution of enantiomers of model compounds [Mosher's acid (3) and its n-Bu₄N salt (4)] (guests) by (+)-dehydroabietyl-N,N-dimethylmethanamine (5) and its